Dual-Element Effects in Pigeons’ Matching-to-Sample with Temporal and Visual Stimuli

The present study examined whether the dual-element effect occurs when temporal and visual stimuli appear simultaneously in a zero-delayed, symbolic matching-to-sample task. Two groups of pigeons were first exposed to either a red or green sample stimulus, for either 30 s or 5 s. The sample was followed by the presentation of yellow and blue comparisons. For pigeons in one group, the duration of the sample was the relevant cue. Responses to the yellow comparison were reinforced if the sample was 30 s, and responses to the blue comparison were reinforced if the sample was 5 s. For the other group, sample duration was irrelevant. Responses to the yellow comparison were reinforced if the sample had been green and responses to the blue comparison were reinforced if the sample had been red. Both groups then learned a second matching task in which the sample and comparison stimuli were vertical and horizontal lines. Finally, matching performance was examined when the lines appeared together with the temporal or color elements. The results showed that the line matching task was acquired more slowly for pigeons that were first trained to attend to duration. More importantly, matching was reduced when the temporal and line elements appeared simultaneously, and the effects were similar to those obtained when visual elements are combined.

     

Control of observing by antecedent stimuli

Five pigeons were run on a one-key discrete trials observing procedure. Trial onset was signaled by a white or yellow key light. Pecks in white or yellow intermittently produced S⁺ and S⁻, green and red key lights that signaled whether the trial would end with response-independent grain reinforcement or nonreinforcement. In the Redundant conditions, white and yellow were correlated with trial outcome, making S⁺ and S⁻ redundant. In the Informative condition, white and yellow were uncorrelated with trial outcome, so that S⁺ and S⁻ provided new information. During the Informative condition, all birds responded in the formerly positive, now uncorrelated color at higher rates than they did during the preceding or succeeding Redundant conditions, in which that same color was positively correlated with primary reinforcement. This result confirmed the prediction that an animal will observe at higher rates in the absence of reinforcement-correlated cues than in their presence.     

Further studies of the McCollough effect

Following prolonged viewing of black and white striped pattems in colored light, red and green aftereffects that lasted as long as 3 days were seen on the patterns, illuminated with white light. Altemate exposures of a vertical pattern of stripes in green light and a horizontal in white light (or a vertical in white light and a horizontal in red light) produced a red aftereffect on the vertical pattern and a green on the horizontal. The red and green aftereffects were also produced with a single vertical pattern. Adaptation colors that were at all greenish produced a red aftereffect on a vertical pattern and a green on a horizontal, whereas colors that were at all reddish produced a green aftereffect on a vertical pattern and a red on a horizontal. Colors near pure blue and pure yellow, which had little red or green content, produced weak aftereffects. The saturation of the aftereffects on the vertical grating varied in proportion to the red or green content of the adaptation color. Vivid red and green aftereffects were frequently obtained with the vertical and horizontal adaptation patterns paired with colors that closely bracketed pure yellow or pure blue. In all cases, the aftereffects gradually desaturated as the head was gradually tilted down to the side; the colors on each test pattern, vertical and horizontal, vanished at 45-deghead tilt and reversed beyond 45 deg.     

The effect of sample duration and cue on a double temporal discrimination

To test the assumptions of two models of timing, Scalar Expectancy Theory (SET) and Learning to Time (LeT), nine pigeons were exposed to two temporal discriminations, each signaled by a different cue. On half of the trials, pigeons learned to choose a red key after a 1.5-s horizontal bar and a green key after a 6-s horizontal bar; on the other half of the trials, they learned to choose a blue key after a 6-s vertical bar and a yellow key after a 24-s vertical bar. During subsequent test trials, they were exposed to the horizontal or vertical bar, for durations ranging from 1.5 to 24 s, and given a choice between novel key combinations: red vs. yellow, or green vs. blue. Results showed a strong effect of sample duration—as the test signal duration increased, preference for green over blue increased and preference for red over yellow decreased. The effect of sample cue was obtained only on the green-blue test trials. These effects are discussed in light of SET and LeT.     

Short-term remembering of discriminative stimuli in pigeons.

Pigeons learned to peck the left or right of two white keys depending on whether a red or a green stimulus was displayed on a third key. The opportunity to peck the white keys was then dealyed for zero to six seconds after the red or green (to-be-remembered) stimulus. On half the trials, the feeder operated during the delay to interrupt behavior that might mediate discriminated responding. No events were scheduled on the remaining trials. In a later condition, the pigeons had the opportunity to peck the white keys during the delay. In general, accuracy decreased as delay increased in all conditions, but performance was least accurate following feeder operations and most accurate when pecking was allowed during the delay. The procedures may be analogous to varying the opportunity for rehearsal in studies of human short-term memory.     

Colored aftereffects produced with moving edges

Colored aftereffects that lasted as long as 6 weeks were produced with moving patterns of parallel black and white stripes or with black and white spirals. During adaptation, the patterns moved periodically in opposite directions, each direction paired with one illuminant, red or green. When the moving patterns were later viewed in white light, S saw the red and green colors, but they were related in the opposite way to the direction of motion. The red and green aftereffects were also produced by other pairs of illuminants, red and white, white and green, reddish-yellow and white, and white and greenish-yellow. The aftereffects did not occur unless, during adaptation, the stripes moved in both directions, each direction paired with a different color. The aftereffect was elicited by stripe motion over the retina—it was seen when the eye swept over a pattern of stationary stripes. The aftereffect desaturated when the retinal orientation of the stripes was changed from the adaptation orientation. Saturation was increased by longer exposure and slower speed during adaptation and by faster speed and a more rapid rate of altemation during the test. The luminance of the adaptation light seemed to have little effect. The aftereffect did not transfer from one eye to the other, and it did not change retinal locus, as was shown when clear images of a colored square that lasted several days were produced with a spiral. S ftxated the spiral’s center. The spiral rotated altemately in opposite directions. A red square with a green surround was projected on the center of the spiral when it rotated in one direction; a green square with a red surround was used when it rotated in the other direction. Following 50 min of adaptation, colored images of the squares were seen when the center of the spiral was ftxated and the direction of     

Effects of two procedures for varying information transmission on observing responses

Two experiments were conducted with pigeons to examine the effects of procedures that varied information transmission on observing responses. The basic procedure for Experiment I was one in which a trial terminated in either non-contingent reinforcement or timeout. Pecking during a trial produced either green (positive) or red (negative) keylights. If no pecking occurred no differential stimuli appeared. The probability of positive trials was either 0.25, 0.50, or 0.75. Observing response rates and relative frequencies of occurrence were highest when the probability of positive trials was 0.25 and lowest at 0.75. In Experiment II, a modified chain procedure was used in which responding produced either red or green lights. Reinforcement or timeout followed light onset by 15 sec. The correlation between the stimuli and the event at the end of the trial (reinforcement or timeout) was varied. Reinforcement followed green 100%, 90%, 70%, or 50% of the time that green occurred. Since the overall probability of reinforcement remained at 0.50, reinforcement followed red in either 0%, 10%, 30%, or 50% of the time that it occurred. The rate of responses that produced these stimuli varied as a function of the correlation. The greater the probability of reinforcement after green, the higher the response rate.     

Choice with delayed and probabilistic reinforcers: effects of variability, time between trials, and conditioned reinforcers.

In a discrete-trials procedure with pigeons, a response on a green key led to a 4-s delay (during which green houselights were lit) and then a reinforcer might or might not be delivered. A response on a red key led to a delay of adjustable duration (during which red houselights were lit) and then a certain reinforcer. The delay was adjusted so as to estimate an indifference point--a duration for which the two alternatives were equally preferred. Once the green key was chosen, a subject had to continue to respond on the green key until a reinforcer was delivered. Each response on the green key, plus the 4-s delay that followed every response, was called one "link" of the green-key schedule. Subjects showed much greater preference for the green key when the number of links before reinforcement was variable (averaging four) than when it was fixed (always exactly four). These findings are consistent with the view that probabilistic reinforcers are analogous to reinforcers delivered after variable delays. When successive links were separated by 4-s or 8-s "interlink intervals" with white houselights, preference for the probabilistic alternative decreased somewhat for 2 subjects but was unaffected for the other 2 subjects. When the interlink intervals had the same green houselights that were present during the 4-s delays, preference for the green key decreased substantially for all subjects. These results provided mixed support for the view that preference for a probabilistic reinforcer is inversely related to the duration of conditioned reinforcers that precede the delivery of food.     

Reciprocal response interactions in concurrent variable-interval and discrete-trial fixed-ratio schedules

Abstract.— Pecking a red key by pigeons was reinforced with grain on a continuously accessible variable-interval schedule. Pecking a second key was reinforced on a discrete-trial fixed-ratio schedule; occasionally the second key was illuminated green and after a single run on the fixed-ratio schedule a reinforcer was presented and the green light was turned off. The experiment investigated the effects of acquisition, extinction, and re-acquisition of pecking the second key. All pigeons changed over immediately from pecking the red key to pecking the green key whenever the green light controlled a high rate of pecking this key. Pecking the red key was completely suppressed during pecking the green key. The experiment shows that a changeover from one response to a second response can come under discriminative control of a stimulus during which the second response is intermittently reinforced. All pigeons frequently emitted observing and orienting behaviors towards the dark key that was occasionally lit green.     

Attention in the pigeon: a reevaluation

During training sessions, pigeons were successively exposed to compounds consisting of a white triangle on a red background and a white circle on a green background. Key pecking intermittently produced grain reinforcers in the presence of one form-color compound. Once key pecking was confined to the compound associated with reinforcement, the elements—red, green, triangle, and circle—were presented during a test in which no reinforcement was available. Each bird pecked nearly exclusively in the presence of the color previously associated with reinforcement, a result that might be interpreted as indicating that the subjects had attended to color, but not form during training. Pecking was next reinforced when either the triangle or the circle was present. Pecking in the presence of the form previously associated with reinforcement was acquired more rapidly. This result suggests that the birds had learned about the forms during training, and that conclusions about attention based on the lack of differential pecking in the nonreinforcement test may not be appropriate.     

Control of pigeons' matching-to-sample performance by differential sample response requirements

Pigeons were trained on a matching-to-sample task in which sample hue and required sample-specific observing behavior provided redundant, relevant cues for correct choices. On trials that involved red and yellow hues as comparison stimuli, a fixed-ratio 16 schedule (FR 16) was required to illuminate the comparisons when the sample was red, and a differential-reinforcement-of-low-rates 3-sec schedule (DRL 3-sec) was required when the sample was yellow. On trials involving blue and green hues as comparison stimuli, an FR 16 schedule was required when the sample was blue and a DRL 3-sec schedule was required when the sample was green. For some pigeons, a 0-sec delay intervened between sample offset and comparison onset, whereas other pigeons experienced a random mixture of 0-sec and 2-sec delay trials. Test trial performance at 0-sec delay indicated that sample-specific behavior controlled choice performance considerably more than sample hue did. Test performance was independent of whether original training involved all 0-sec delay trials or a mixture of 0-sec and 2-sec delays. Sample-specific observing response requirements appear to facilitate pigeons' matching-to-sample performance by strengthening associations between the observing response and correct choice.     

Substitution effects in a generalized token economy with pigeons

Pigeons made repeated choices between earning and exchanging reinforcer‐specific tokens (green tokens exchangeable for food, red tokens exchangeable for water) and reinforcer‐general tokens (white tokens exchangeable for food or water) in a closed token economy. Food and green food tokens could be earned on one panel; water and red water tokens could be earned on a second panel; white generalized tokens could be earned on either panel. Responses on one key produced tokens according to a fixed‐ratio schedule, whereas responses on a second key produced exchange periods, during which all previously earned tokens could be exchanged for the appropriate commodity. Most conditions were conducted in a closed economy, and pigeons distributed their token allocation in ways that permitted food and water consumption. When the price of all tokens was equal and low, most pigeons preferred the generalized tokens. When token‐production prices were manipulated, pigeons reduced production of the tokens that increased in price while increasing production of the generalized tokens that remained at a fixed price. The latter is consistent with a substitution effect: Generalized tokens increased and were exchanged for the more expensive reinforcer. When food and water were made freely available outside the session, token production and exchange was sharply reduced but was not eliminated, even in conditions when it no longer produced tokens. The results join with other recent data in showing sustained generalized functions of token reinforcers, and demonstrate the utility of token‐economic methods for assessing demand for and substitution among multiple commodities in a laboratory context.     

The role of preliminary magazine training in acquisition of the autoshaped key peck

A series of experiments tested the hypothesis that initial key pecks in the autoshaping procedure are generalized pecks at the illuminated grain hopper. Experiment I found that autoshaping readily occurred when the chamber was continuously illuminated by a house-light. In Experiment II, pigeons given magazine training and autoshaping with an unlighted grain hopper failed to autoshape in 200 trials. Acquisition of autoshaped key pecking was retarded in Experiment III when stimulus control by the magazine light was reduced. In the fourth study, pigeons were given magazine training with either a red or white magazine light and then given autoshaping with concurrently presented red and white keys. For all pigeons in this experiment, the first key peck occurred on the key of the same color as that pigeon's magazine light. The results of these experiments were interpreted as supporting an account of autoshaping that identifies initial key pecks as arising due to generalization of pecking at the lighted grain hopper to pecking at the lighted key.     

Duration comparison: relative stimulus differences stimulus age, and stimulus predictiveness.

Under a psychophysical trials procedure, pigeons were presented with a red light of one duration followed by a green light of a second duration. Eight geometrically spaced base durations were paired with one of four shorter and four longer durations as the alternate member of a duration pair, with different pairs randomly intermixed. One choice was reinforced if red had lasted longer than green, and a second choice was reinforced if green had lasted longer. Performance was compared when all the base durations and their pair members were included (entire-range condition) or when only the four longest base durations and their comparison durations (restricted-range condition) were used. Discrimination sensitivity decreased for longer duration pairs under both conditions, supporting a memory-based account. Sensitivity was lower under the restricted-range condition. Under both conditions, a bias to report "green as longer" increased as the second green duration increased. Bias changed as a matching function of the green-duration predictiveness of the correct choice. The results are related to a quantitative model of timing and remembering proposed by Staddon.     

Response-rate invariance in concurrent schedules: effects of different changeover contingencies

In a two-key chamber, one key (the food key) was either red or green with different variable-interval schedules operating concurrently in each color and a second key (the changeover key) served to change the food-key color. Three pigeons were trained with either a 2-sec changeover delay or a 0-sec changeover delay and three birds with a fixed-ratio 2 on the changeover key instead of a changeover delay. The proportion of time spent in red approximated the proportion of reinforcers delivered in red for all birds. When the procedure was changed so that reinforcers were signalled in the green schedule, rates of reinforcement were unaltered, but the pigeons spent virtually the whole session in red. Changeovers to green were allowed only when a reinforcer was assigned by the schedule associated with green. For all pigeons with the fixed–ratio requirement on the changeover key or with a 0-sec changeover delay, the overall rate of red-key responses was higher during the signalling condition than during unsignalled, or baseline, condition. The present data question the generality of previous reports that the rate of one response is independent of the amount of time allocated to the alternative response.     

Punishment of observing by the negative discriminative stimulus

To determine the effect of a negative discriminative stimulus on the response producing it, two pigeons were each studied in a three-key conditioning chamber. During alternating periods of unpredictable duration, pecking the center (food) key either was reinforced with grain on a variable-interval schedule or was never reinforced. On equal but independent variable-interval schedules, pecking either of the side (observing) keys changed the color of all keys for 30 sec from yellow to either green or red. When the schedule on the center key was variable-interval reinforcement, the color was green (positive discriminative stimulus); when no reinforcements were scheduled, the color was red (negative discriminative stimulus). Since pecking the side keys did not affect grain deliveries, changes in the rate of pecking could not be ascribed to changes in the frequency of primary reinforcement. In subsequent sessions, red was withheld as one of the possible consequences of pecking a given side key. When red was omitted, the rate on that key increased, and when red was restored, the rate decreased. It was concluded that red illumination of the keys, the negative discriminative stimulus, had a suppressive effect on the response that produced it.     

Conditioned reinforcement and choice with delayed and uncertain primary reinforcers.

In an adjusting-delay choice procedure, pigeons could peck on either a red key or a green key. A peck on the red key always led to a delay associated with red houselights and then food. The delay was adjusted over trials to estimate an indifference point--a delay at which the two keys were chosen about equally often. In some conditions, a peck on the green key led to food on all trials after delays of either 10 s or 30 s, and green houselights were lit during the delays. In other conditions, food was presented on only half of the green-key trials. If the green houselights continued to occur on both reinforcement and nonreinforcement trials, preference for the green key always decreased. Preference for the green key also decreased if half of the trials had 30-s houselights followed by food and the other half had no green houselights and no food. However, preference for the green key actually increased if half of the trials had 10-s green houselights followed by food and the other half had no green houselights followed by no food. The latter condition therefore demonstrated a case in which preference for an alternative increased when food was removed from half of the trials. The results suggest that the red and green houselights served as conditioned reinforcers. A hyperbolic decay model (Mazur, 1989) provided good predictions for all conditions by assuming that the strength of a conditioned reinforcer is inversely related to the total time spent in its presence before food is delivered.     

On conditioned reinforcing effects of negative discriminative stimuli

Observing responses by pigeons were studied during sessions in which a food key and an observing key were available continuously. A variable-interval schedule and extinction alternated randomly on the food key. In one condition, food-key pecking during extinction decreased reinforcement frequency during the next variable-interval component, and in the other condition such pecking did not affect reinforcement frequency. Observing responses either changed both keylight colors from white to green (S+) or to red (S−) depending on the condition on the food key, or the observing responses never produced the S+ but produced the S− when extinction was in effect on the food key. Observing responses that produced only S− were maintained only when food-key pecking during extinction decreased reinforcement frequency in the subsequent variable-interval component. The red light conformed to conventional definitions of a negative discriminative stimulus, rendering results counter to previous findings that production of S− alone does not maintain observing. Rather than offering support for an informational account of conditioned reinforcement, the results are discussed in terms of a molar analysis to account for how stimuli acquire response-maintaining properties.     

3—6岁白、哈尼族与汉族儿童的颜色命名能力的发展

探讨了云南地区白族与哈尼族３—６岁儿童的颜色命名能力发展,并与北京地区汉族同龄儿童作了比较。实验结果表明,不同民族的儿童的颜色命名能力都伴随年龄增长而逐步提高;但汉族儿童的颜色命名能力发展略高于哈尼族与白族同龄儿童。总的来看,儿童对不同颜色正确命名能力的发展有着共同的规律性,即黑、白、红三色较易正确命名,其次是黄、绿、蓝三色较难正确命名,命名正确率最低的颜色是橙与紫。